Sodium Sulfate, Potassium Sulfate, and Magnesium Sulfate Bowel Prep kit
Active substance: SODIUM SULFATE ANHYDROUS, POTASSIUM SULFATE, MAGNESIUM SULFATE, UNSPECIFIED FORM
SOLUTION · SODIUM SULFATE ANHYDROUS 17.5 g/177mL, POTASSIUM SULFATE 3.13 g/177mL, MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/177mL
United StatesActive
Marketing holder: Sun Pharmaceutical Industries, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- SODIUM SULFATE ANHYDROUS · 17.5 g/177mL
- POTASSIUM SULFATE · 3.13 g/177mL
- MAGNESIUM SULFATE, UNSPECIFIED FORM · 1.6 g/177mL
Registration
- Registration number
- 51672-4170
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 51672-4170 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 51672-4170 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 51672-4170 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 51672-4170 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 51672-4170 · Verified 2026-10-09 · open in source